LymphedemaV1, Main, Exploration, bibRecord, 007621

Early fetal death associated with compound heterozygosity for Noonan syndrome‐causative PTPN11 mutations

Identifieur interne : 007621 ( Main/Exploration ); précédent : 007620; suivant : 007622

Early fetal death associated with compound heterozygosity for Noonan syndrome‐causative PTPN11 mutations

Auteurs : Kristin Becker [Royaume-Uni] ; Helen Hughes [Royaume-Uni] ; Karol Howard [Royaume-Uni] ; Maggie Armstrong [Royaume-Uni] ; Devender Roberts [Royaume-Uni] ; Edgar J. Lazda [Royaume-Uni] ; John P. Short [Royaume-Uni] ; Adam Shaw [Royaume-Uni] ; Michael A. Patton [Royaume-Uni] ; Marco Tartaglia [Italie]

Source :

American Journal of Medical Genetics Part A [ 1552-4825 ] ; 2007-06-01.

RBID : ISTEX:5D0222BFBCAA90C25456ECCC421C78BD5F1D132F
Url:

https://api.istex.fr/document/5D0222BFBCAA90C25456ECCC421C78BD5F1D132F/fulltext/pdf

DOI: 10.1002/ajmg.a.31738

Affiliations:

Links toward previous steps (curation, corpus...)

to stream Istex, to step Corpus: 002B44
to stream Istex, to step Curation: 002B44
to stream Istex, to step Checkpoint: 001467
to stream Main, to step Merge: 007774
to stream Main, to step Curation: 007621

Le document en format XML

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<author><name sortKey="Hughes, Helen" sort="Hughes, Helen" uniqKey="Hughes H" first="Helen" last="Hughes">Helen Hughes</name>
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<author><name sortKey="Howard, Karol" sort="Howard, Karol" uniqKey="Howard K" first="Karol" last="Howard">Karol Howard</name>
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<author><name sortKey="Armstrong, Maggie" sort="Armstrong, Maggie" uniqKey="Armstrong M" first="Maggie" last="Armstrong">Maggie Armstrong</name>
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<author><name sortKey="Roberts, Devender" sort="Roberts, Devender" uniqKey="Roberts D" first="Devender" last="Roberts">Devender Roberts</name>
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<author><name sortKey="Lazda, Edgar J" sort="Lazda, Edgar J" uniqKey="Lazda E" first="Edgar J." last="Lazda">Edgar J. Lazda</name>
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<author><name sortKey="Short, John P" sort="Short, John P" uniqKey="Short J" first="John P." last="Short">John P. Short</name>
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<author><name sortKey="Shaw, Adam" sort="Shaw, Adam" uniqKey="Shaw A" first="Adam" last="Shaw">Adam Shaw</name>
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<author><name sortKey="Patton, Michael A" sort="Patton, Michael A" uniqKey="Patton M" first="Michael A." last="Patton">Michael A. Patton</name>
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<author><name sortKey="Tartaglia, Marco" sort="Tartaglia, Marco" uniqKey="Tartaglia M" first="Marco" last="Tartaglia">Marco Tartaglia</name>
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<author><name sortKey="Roberts, Devender" sort="Roberts, Devender" uniqKey="Roberts D" first="Devender" last="Roberts">Devender Roberts</name>
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<wicri:regionArea>Fetal Centre, Liverpool Women's Hospital, Liverpool</wicri:regionArea>
<wicri:noRegion>Liverpool</wicri:noRegion>
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<name sortKey="Becker, Kristin" sort="Becker, Kristin" uniqKey="Becker K" first="Kristin" last="Becker">Kristin Becker</name>
<name sortKey="Becker, Kristin" sort="Becker, Kristin" uniqKey="Becker K" first="Kristin" last="Becker">Kristin Becker</name>
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<country name="Italie"><region name="Latium"><name sortKey="Tartaglia, Marco" sort="Tartaglia, Marco" uniqKey="Tartaglia M" first="Marco" last="Tartaglia">Marco Tartaglia</name>
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Early fetal death associated with compound heterozygosity for Noonan syndrome‐causative PTPN11 mutations

Early fetal death associated with compound heterozygosity for Noonan syndrome‐causative PTPN11 mutations

Source :

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri